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- R+D & Community of Interest
Update of VDI 2083 Sheet 21: Derivation of acceptance criteria for product-specific purity requirements
Purity of medical devices in the manufacturing process
The determination of the purity of medical devices has been uniformly regulated since October of this year: VDI Guideline 2083 Sheet 21 offers guidance on how manufacturers can determine whether purity limits are necessary for their products and how these can be derived and verified. The next, consi…








